Dichotomy of protective cellular immune responses to human visceral leishmaniasis

Author:

Khalil E A G1,Ayed N B1,Musa A M1,Ibrahim M E1,Mukhtar M M1,Zijlstra E E1,Elhassan I M1,Smith P G2,Kieny P M3,Ghalib H W3,Zicker F3,Modabber F4,Elhassan A M1

Affiliation:

1. The Leishmaniasis Research Group/Sudan: Institute of Endemic Diseases, University of Khartoum, Khartoum

2. London School of Hygiene and Tropical Medicine, Keppel Street, London, UK

3. TDR/WHO, Geneva, Switzerland

4. Infectious Diseases Research Institute, Seattle, USA

Abstract

Summary Healing/protective responses in human visceral leishmaniasis (VL) are associated  with  stimulation/production  of  Th1  cytokines,  such  as  interferon IFN-γ, and conversion in the leishmanin skin test (LST). Such responses were studied for 90 days in 44 adult healthy volunteers from VL non-endemic areas, with no past history of VL/cutaneous leishmaniasis (CL) and LST non-reactivity following injection with one of four doses of Alum-precipitated autoclaved Leishmania major (Alum/ALM) ± bacille Calmette–Guérin (BCG), a VL candidate vaccine. The vaccine was well tolerated with minimal localized side-effects and without an increase in antileishmanial antibodies or interleukin (IL)-5. Five volunteers (5/44; 11·4%) had significant IFN-γ production by peripheral blood mononuclear cells (PBMCs) in response to Leishmania antigens in their prevaccination samples (P = 0·001) but were LST non-reactive. On day 45, more than half the volunteers (26/44; 59·0%) had significantly high LST indurations (mean 9·2 ± 2·7 mm) and high IFN-γ levels (mean 1008 ± 395; median 1247 pg/ml). Five volunteers had significant L. donovani antigen-induced IFN-γ production (mean 873 ± 290; median 902; P = 0·001), but were non-reactive in LST. An additional five volunteers (5/44; 11·4%) had low IFN-γ levels (mean 110 ± 124 pg/ml; median 80) and were non-reactive in LST (induration = 00 mm). The remaining eight volunteers had low IFN-γ levels, but significant LST induration (mean 10 ± 2·9 mm; median 11). By day 90 the majority of volunteers (27/44; 61·4%) had significant LST induration (mean 10·8 ± 9·9 mm; P < 0·001), but low levels of L. donovani antigen-induced IFN-γ (mean 66·0 ± 62 pg/ml; P > 0.05). Eleven volunteers (11/44; 25%) had significantly high levels of IFN-γ and LST induration, while five volunteers had low levels of IFN-γ (<100 pg/ml) and no LST reactivity (00 mm). One volunteer was lost to follow-up. In conclusion, it is hypothesized that cellular immune responses to human VL are dichotomatous, and that IFN-γ production and the LST response are not in a causal relationship. Following vaccination and probably cure of VL infection, the IFN-γ response declines with time while the LST response persists. LST is a simple test that can be used to assess candidate vaccine efficacy.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

Reference22 articles.

1. Diversity among Leishmania isolates from the Sudan: isoenzyme homogeneity of L. donovani versus heterogeneity of L. major;Ibrahim;Trans R Soc Trop Med Hyg,1995

2. Risk mapping of visceral leishmaniasis: the role of local variation in rainfall and altitude on the presence and incidence of kala-azar in eastern Sudan;Elnaiem;Am J Trop Med Hyg,2003

3. Leishmaniasis in Sudan;El-Hassan;Trans R Soc Trop Med Hyg,2001

4. Characterization of the humoral immune response in Sudanese leishmaniasis: specific antibody detected by class- and subclass-specific reagents;El Amin;Clin Exp Immunol,1986

5. Immunoblot analysis of the humoral immune response to Leishmania donovani polypeptides in cases of human visceral leishmaniasis: its usefulness in prognosis;Kumar;Clin Diag Lab Immunol,2002

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